Literature DB >> 21240560

Impact of computer-assisted data collection, evaluation and management on the cancer genetic counselor's time providing patient care.

Stephanie A Cohen1, Dawn E McIlvried.   

Abstract

Cancer genetic counseling sessions traditionally encompass collecting medical and family history information, evaluating that information for the likelihood of a genetic predisposition for a hereditary cancer syndrome, conveying that information to the patient, offering genetic testing when appropriate, obtaining consent and subsequently documenting the encounter with a clinic note and pedigree. Software programs exist to collect family and medical history information electronically, intending to improve efficiency and simplicity of collecting, managing and storing this data. This study compares the genetic counselor's time spent in cancer genetic counseling tasks in a traditional model and one using computer-assisted data collection, which is then used to generate a pedigree, risk assessment and consult note. Genetic counselor time spent collecting family and medical history and providing face-to-face counseling for a new patient session decreased from an average of 85-69 min when using the computer-assisted data collection. However, there was no statistically significant change in overall genetic counselor time on all aspects of the genetic counseling process, due to an increased amount of time spent generating an electronic pedigree and consult note. Improvements in the computer program's technical design would potentially minimize data manipulation. Certain aspects of this program, such as electronic collection of family history and risk assessment, appear effective in improving cancer genetic counseling efficiency while others, such as generating an electronic pedigree and consult note, do not.

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Year:  2011        PMID: 21240560     DOI: 10.1007/s10689-011-9417-2

Source DB:  PubMed          Journal:  Fam Cancer        ISSN: 1389-9600            Impact factor:   2.375


  19 in total

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3.  Routine history as compared to audio computer-assisted self-interview for prenatal care history taking.

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4.  Efficacy of a touchscreen computer based family cancer history questionnaire and subsequent cancer risk assessment.

Authors:  J Westman; H Hampel; T Bradley
Journal:  J Med Genet       Date:  2000-05       Impact factor: 6.318

5.  Prevalence of hereditary breast/ovarian carcinoma risk in patients with a personal history of breast or ovarian carcinoma in a mammography population.

Authors:  Francisco J Dominguez; Julie L Jones; Katherina Zabicki; Barbara L Smith; Michele A Gadd; Michele Specht; Daniel B Kopans; Richard H Moore; James S Michaelson; Kevin S Hughes
Journal:  Cancer       Date:  2005-11-01       Impact factor: 6.860

6.  Assessment of clinical practices among cancer genetic counselors.

Authors:  Deborah Wham; Thuy Vu; Gayun Chan-Smutko; Christine Kobelka; Diana Urbauer; Brandie Heald
Journal:  Fam Cancer       Date:  2010-09       Impact factor: 2.375

7.  Education about genetic testing for breast cancer susceptibility: patient preferences for a computer program or genetic counselor.

Authors:  M J Green; A M McInerney; B B Biesecker; N Fost
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8.  Patient's perceptions of an anesthesia preoperative computerized patient interview.

Authors:  S A Vitkun; J G Halpern-Lewis; S A Williams; J S Gage; P J Poppers
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9.  Prevalence of family history of breast and ovarian cancer in a single primary care practice using a self-administered questionnaire.

Authors:  Kevin S Hughes; Constance Roche; Curtis T Campbell; Nancy Siegel; Lisa Salisbury; Amy Chekos; Maya S Katz; Erica Edell
Journal:  Breast J       Date:  2003 Jan-Feb       Impact factor: 2.431

10.  The practice of clinical genetics: a survey of practitioners.

Authors:  Beth A Pletcher; Ethan A B Jewett; William L Cull; Sarah E Brotherton; H Eugene Hoyme; Richard J D Pan; Holly J Mulvey
Journal:  Genet Med       Date:  2002 May-Jun       Impact factor: 8.822

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  6 in total

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Journal:  J Genet Couns       Date:  2014-08-15       Impact factor: 2.537

2.  Initial clinical validation of Health Heritage, a patient-facing tool for personal and family history collection and cancer risk assessment.

Authors:  Leigh A Baumgart; Kristen J Vogel Postula; William A Knaus
Journal:  Fam Cancer       Date:  2016-04       Impact factor: 2.375

Review 3.  A clinical approach to inherited hypertrophy: the use of family history in diagnosis, risk assessment, and management.

Authors:  Kyla E Dunn; Colleen Caleshu; Allison L Cirino; Carolyn Y Ho; Euan A Ashley
Journal:  Circ Cardiovasc Genet       Date:  2013-02

4.  Providing patient education: impact on quantity and quality of family health history collection.

Authors:  Chris A Beadles; R Ryanne Wu; Tiffany Himmel; Adam H Buchanan; Karen P Powell; Elizabeth Hauser; Vincent C Henrich; Geoffrey S Ginsburg; Lori A Orlando
Journal:  Fam Cancer       Date:  2014-06       Impact factor: 2.375

5.  An internal performance assessment of CancerGene Connect: an electronic tool to streamline, measure and improve the genetic counseling process.

Authors:  Mary Pritzlaff; Arielle Yorczyk; Linda S Robinson; Sara Pirzadeh-Miller; Tirun Lin; David Euhus; Theodora S Ross
Journal:  J Genet Couns       Date:  2014-06-12       Impact factor: 2.537

Review 6.  The composition and capacity of the clinical genetics workforce in high-income countries: a scoping review.

Authors:  Nick Dragojlovic; Kennedy Borle; Nicola Kopac; Ursula Ellis; Patricia Birch; Shelin Adam; Jan M Friedman; Amy Nisselle; Alison M Elliott; Larry D Lynd
Journal:  Genet Med       Date:  2020-06-24       Impact factor: 8.822

  6 in total

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